A Radiolabeled Photoswitchable G Protein-Coupled Receptor Antagonist Enlightens Ligand Binding Kinetics Associated with Photoswitching

放射性标记的光开关G蛋白偶联受体拮抗剂揭示了与光开关相关的配体结合动力学

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Abstract

Photopharmacology offers powerful opportunities to control protein signaling using photoresponsive ligands. Despite the vast potential of photoswitchable ligands for spatiotemporal target protein control, research on ligand-protein binding kinetics of these ligands remains limited. Herein, we describe the discovery of the first radiolabeled photoswitchable ligand, [(3)H]VUF26063 ([(3)H]3f), to assess light-dependent ligand-protein binding kinetics in real time. The key compound (3f) is an arylazopyrazole-based antagonist targeting a prototypic family A G protein-coupled receptor (GPCR), the histamine H(3) receptor (H(3)R), and enabled convenient radiolabeling via a growth vector on the pyrazole. Its photochemical properties, subnanomolar affinity of the trans isomer and a 50-fold decrease in affinity upon switching, allowed for reversible photochemical control of H(3)R binding kinetics in real time. The kinetic binding data obtained with this radiolabeled ligand indicate that 3f isomerizes in the H(3)R extended binding pocket upon illumination. Our results shed light on the binding kinetics of photoswitchable ligands and will have relevance beyond GPCRs as targets.

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